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Stryker Hip Lawyers Mississippi - Toll Free 1-866-777-2557

Stryker Hip Lawyer Mississippi - Stryker Hip Replacement Lawyer Mississippi

If you or a loved one had hip replacement surgery and are experiencing certain side effects like metal poisoning or the need for a second revision surgery, you may be entitled to financial compensation from the manufacturer. Call us today to get the facts.  Call Toll Free 1-866-777-2557 or fill out our online contact form below and a Mississippi Stryker Hip Implant Lawyer will get back to you as soon as possible.   This is a free, no obligation consultation. There are no legal fees unless we make a recovery for you.  Time is limited, so please call today.

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We are investigating cases involving:

DePuy ASR Hip Recall
DePuy Pinnacle Hip Lawsuit
Wright Conserve Hip Cup
Wright Conserve Plus Lawsuit
Zimmer Durom Cup Hip Implant
Smith & Nephew R3 Acetabular System
Wright Profemur Z Hip Replacement
Stryker Rejuvenate

Stryker ABG II Modular Neck Stems

​Stryker LFIT Anatomic V40 Femoral Head

Cobalt Poisoning

Chromium Poisoning


Stryker Hip Lawyer Mississippi

FDA Against Recommending the Use of Metal-on-Metal Hip Replacements
In recent times, metal-on-metal hip implant products have been confronted with plenty of recalls as well as raised buyer distress with the safeness of these products. Several top developers of such models, comprising of Stryker, DePuy, as well as Smith & Nephew, have ordered back its metal-on-metal hip augmentations and today face legal actions with people seeking remuneration intended for sufferings due to these models.

On a metal-on-metal hip implant model, the pieces on the system are manufactured from a variety of metals - most ordinarily, the cobalt-chromium-molybdenum alloy combination. As the portions and conjunctions on the metallic components rub together, tearing away on the parts could discharge metal remains to the joint region. Preliminary indicators of this issue feature boosted joint soreness along with minimal movability.

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Under serious circumstances, such metallic contaminants can cause an issue named as metallosis (metal positioning). This occurs if chromium or cobalt ions go into the individual's blood circulation and starts a systemic reaction to the poisonous amounts of metal. For many of these individuals, complex modification surgical procedure is the only alternative to receive respite from the indicators involving metallosis.

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FDA Recommendations for Metal Hip Augmentations
The FDA has resolved client trouble to the dangers of metal-on-metal hip alternatives, and they have issued a lot of protection notifications concerning these devices. Also, the FDA has put together particular recommendations for orthopedic physicians and people that have obtained a metal-on-metal hip enhancement. These suggestions feature:

• Habitual clinical examination - with increased consistent sessions involving symptomatic clients
• Soft tissue imaging for people suffering from difficulties with their augmentation
• Metallic ion testing for symptomatic patients using a metal augmentation
• Averting the utilization of metal-on-metal enhancements for certain demographics that have heightened danger
• Extensive individual counseling about the risks of metal implants before surgery

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There are specific people that research has shown with an enhanced possibility of creating complications with a metal hip replacement. Due to this, the FDA suggests that doctors will not set up this kind of product in these clients. Higher risk populations contain patients with serious renal insufficiency, metal sensitivity, and subdued immunity defenses. Furthermore, metallic enhancements are not recommended for utilization in ladies with childbearing age.

Even though clients are not dealing with troubles linked to metal-on-metal hip enhancements, the FDA endorses that all individuals with a metal augmentation follow-up on their orthopedic surgeon every one to two years in order to be examined with complications. For people that are displaying initial indications of metallosis or other troubles, the FDA recommends that a clinical analysis occur every six months.

Stryker Hip Replacement Lawyer Mississippi

Hip Replacement Lawsuit Lawyers